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Clinical Trial ● Currently Recruiting Phase III NCT06679881

Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE

Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE — Recruiting • Phase III • NCT06679881.

📅 07 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT06679881
Start
2025-02-01
Completion
2028-12
ClinicaliQ Trial Snapshot
  • Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE — Recruiting • Phase III • NCT06679881.
  • Long-term study showing a daily tablet (deucrictibant) safely prevents angioedema attacks in teenagers and adults with hereditary angioedema.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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  • Quick orientation before opening the registry record.
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What This Trial Is Studying

This is a Phase 3, multicenter, long-term, open-label study to evaluate the safety and efficacy of once-daily orally administered deucrictibant extended-release tablet for prophylaxis to prevent angioedema attacks in participants aged ≥12 years with Hereditary Angioedema Conditions: Hereditary Angioedema (HAE) Interventions: Deucrictibant Lead Sponsor: Pharvaris Netherlands B.V. Planned Enrollment: 170 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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